| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87187670-87187710 | Rare:7 | ||||
| chr7:87192450-87192651 | Common:2; Rare:38 | ||||
| chr7:87345097-87345762 | Common:7; Rare:172 | ||||
| chr7:87876124-87876723 | Common:3; Rare:238 | ||||
| chr7:88219980-88220265 | Common:3; Rare:110 | ||||
| chr7:90154378-90154537 | Rare:39 | ||||
| chr7:90211633-90211931 | Common:4; Rare:92 | ||||
| chr7:90245094-90245221 | Rare:39 | ||||
| chr7:90346528-90346752 | Common:4; Rare:97 | ||||
| chr7:90403104-90403539 | Common:3; Rare:100 | ||||
| chr7:90595862-90596091 | Common:6; Rare:82 | ||||
| chr7:90596215-90596401 | Rare:61 | ||||
| chr7:91880658-91880827 | Common:2; Rare:48 | ||||
| chr7:91940735-91941025 | Common:4; Rare:92; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92097318-92097778 | Common:1; Rare:115; Clinvar:4; Clinvar (benign):4 |